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Richard O. Francis Jeffrey Jhang Jeanne E. Hendrickson James C. Zimring Eldad A. Hod Steven L. Spitalnik 《Transfusion》2013,53(3):606-611
BACKGROUND: Glucose‐6‐phosphate dehydrogenase (G6PD) deficiency is characterized by red blood cell (RBC) destruction in response to oxidative stress. Although blood donors are not routinely screened for G6PD deficiency, the transfusion of stored G6PD‐deficient RBCs may have serious adverse outcomes. By measuring G6PD enzyme activity of RBC units from a large metropolitan hospital transfusion service, we sought to determine 1) the prevalence of G6PD‐deficient RBC units, 2) if G6PD activity changes during storage, and 3) if G6PD activity in segments correlates with its activity in the bags. STUDY DESIGN AND METHODS: Quantitative G6PD activity was measured in 301 randomly selected RBC units and 73 D+C?E? (i.e., R0r or R0R0) RBC units, all stored in additive solutions. G6PD deficiency was defined as activity less than 60% of the normal mean. RESULTS: The frequency of G6PD‐deficient units in the general inventory was 0.3% (1/301; 95% confidence interval [CI], <0.01%‐2.1%). In contrast, its frequency in D+C?E? RBC units was 12.3% (9/73; 95% CI, 6.4%‐22.0%). G6PD activity did not significantly change during the 42‐day storage period, and G6PD activity measured in RBC storage bags and attached segments correlated well (r = 0.7‐0.9, p ≤ 0.001, Spearman rank correlation). CONCLUSIONS: Although the frequency of G6PD‐deficient RBC units in the transfusion service general inventory was relatively low, it was significantly higher among a subset of R0r or R0R0 units. The latter are preferentially allocated for transfusion to patients with sickle cell disease to decrease the risk of RBC alloimmunization, possibly allowing more of these units to be inadvertently targeted to these patients. 相似文献
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目的:根据湿润暴露疗法的基本理论,探讨MEBT/MEBO治疗眼角膜火碱烧伤的作用。方法:应用MEBT/MEBO综合疗法治疗30例(42眼)。结果:患者眼视力均恢复至0.6以上,且角膜清晰可见。结论:打破了传统医学认为眼科治疗关于前弹力层及其实质层损伤后不能再生的传统观念,开创了中西医结合治疗眼角膜火碱烧伤的美好前景。 相似文献
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Yunsook Jhang Jung Ju Lee Jong-Moo Park Ja-Seong Koo Byung-Kun Kim Ohyun Kwon 《JOURNAL OF CLINICAL NEUROLOGY》2007,3(2):116-119
Paraproteinemia potentially causes peripheral neuropathy via an unknown underlying pathogenetic mechanism. We report a case of pathologically proven amyloid neuropathy with AL amyloidosis with an IgA kappa light chain, which was initially diagnosed as neuropathy associated with monoclonal gammopathy of undetermined significance. This case indicates that in cases of neuropathy with paraproteinemia, the other potential causes should be excluded by appropriate means, especially pathological evaluations. 相似文献
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Young A Kim Eun-Ju Ha Won Kyoung Jhang Seong Jong Park 《Intensive care medicine》2013,39(10):1818-1823